Variant report

Variant	esv3338669
Chromosome Location	chr3:67925912-68064160
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:389)
CpG islands
(count:794)
Chromatin interactive
region (count:11)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:67926647-67927182	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:67925864-67926374	HepG2	liver:	n/a	chr3:67926095-67926111 chr3:67926096-67926112
3	BACH1	chr3:68017186-68017276	K562	blood:	n/a	n/a
4	BHLHE40	chr3:67935315-67935332	GM12878	blood:	n/a	n/a
5	CCNT2	chr3:68033067-68033322	K562	blood:	n/a	n/a
6	CEBPB	chr3:67964275-67964462	H1-hESC	embryonic stem cell:	n/a	chr3:67964358-67964369
7	CEBPB	chr3:67985164-67985454	IMR90	lung:	n/a	chr3:67985315-67985326
8	CEBPB	chr3:67964234-67964528	HepG2	liver:	n/a	chr3:67964358-67964369
9	CEBPB	chr3:67985138-67985469	HepG2	liver:	n/a	chr3:67985315-67985326
10	CEBPB	chr3:68030853-68031196	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr3:68030854-68031193	HepG2	liver:	n/a	n/a
12	CEBPB	chr3:67974240-67974550	HepG2	liver:	n/a	n/a
13	CEBPB	chr3:68037007-68037284	H1-hESC	embryonic stem cell:	n/a	chr3:68037159-68037170
14	CEBPB	chr3:68037001-68037283	HepG2	liver:	n/a	chr3:68037159-68037170
15	CEBPB	chr3:67926694-67926991	A549	lung:	n/a	n/a
16	CEBPB	chr3:68037035-68037272	A549	lung:	n/a	chr3:68037159-68037170
17	CEBPB	chr3:67926813-67926954	HepG2	liver:	n/a	n/a
18	CEBPB	chr3:68055781-68055942	HepG2	liver:	n/a	n/a
19	CEBPB	chr3:68033366-68033687	HepG2	liver:	n/a	chr3:68033525-68033536 chr3:68033502-68033513
20	CEBPB	chr3:67980779-67981121	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr3:67926677-67927058	HepG2	liver:	n/a	n/a
22	CEBPB	chr3:67932535-67932706	HepG2	liver:	n/a	chr3:67932573-67932584 chr3:67932639-67932651 chr3:67932571-67932582
23	CEBPB	chr3:67997188-67997474	HepG2	liver:	n/a	chr3:67997344-67997355
24	CEBPB	chr3:68037096-68037312	K562	blood:	n/a	chr3:68037159-68037170
25	CEBPB	chr3:67974289-67974478	A549	lung:	n/a	n/a
26	CEBPB	chr3:67926724-67926973	HepG2	liver:	n/a	n/a
27	CEBPB	chr3:67926670-67927091	HepG2	liver:	n/a	n/a
28	CEBPB	chr3:68037023-68037308	IMR90	lung:	n/a	chr3:68037159-68037170
29	CHD2	chr3:68047488-68047694	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr3:68056739-68057304	H1-hESC	embryonic stem cell:	n/a	chr3:68056886-68056896
31	CHD2	chr3:67998544-67998794	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr3:67991180-67991330	HVMF	connective:	n/a	n/a
33	CTCF	chr3:68057279-68057343	Kidney_OC	kidney:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
34	CTCF	chr3:67952320-67952470	HCT-116	colon:	n/a	n/a
35	CTCF	chr3:67991060-67991210	NHDF-neo	bronchial:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136
36	CTCF	chr3:67952200-67952350	GM12873	blood:	n/a	n/a
37	CTCF	chr3:67998980-67999130	Caco-2	colon:	n/a	n/a
38	CTCF	chr3:67952202-67952416	MCF-7	breast:	n/a	n/a
39	CTCF	chr3:68057180-68057330	SK-N-SH_RA	brain:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
40	CTCF	chr3:67952200-67952350	GM06990	blood:	n/a	n/a
41	CTCF	chr3:68057200-68057350	HAc	cerebellar:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
42	CTCF	chr3:68057182-68057417	Medullo	brain:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
43	CTCF	chr3:67952206-67952414	LNCaP	prostate:	n/a	n/a
44	CTCF	chr3:67952240-67952390	BE2_C	brain:	n/a	n/a
45	CTCF	chr3:67952246-67952366	MCF-7	breast:	n/a	n/a
46	CTCF	chr3:67952220-67952370	K562	blood:	n/a	n/a
47	CTCF	chr3:67952200-67952350	GM12871	blood:	n/a	n/a
48	CTCF	chr3:68057160-68057310	AG04449	skin:	n/a	chr3:68057285-68057293
49	CTCF	chr3:67952147-67952356	T-47D	breast:	n/a	n/a
50	CTCF	chr3:68015842-68015927	Lung_OC	lung:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:68047840-68047890	Jurkat	blood:	n/a
2	chr3:68047840-68047890	Jurkat	blood:	n/a
3	chr3:68057322-68057372	SK-N-SH_RA	brain:	n/a
4	chr3:68056706-68056756	HUVEC	blood vessel:	n/a
5	chr3:68053484-68053534	Hela-S3	cervix:	n/a
6	chr3:68053273-68053323	Jurkat	blood:	n/a
7	chr3:68053273-68053323	HAEpiC	amniotic membrane:	n/a
8	chr3:68047840-68047890	ECC-1	luminal epithelium:	n/a
9	chr3:68039483-68039533	SK-N-SH	brain:	n/a
10	chr3:68057306-68057356	NH-A	brain:	n/a
11	chr3:68057357-68057407	HEEpiC	esophagus:	n/a
12	chr3:68057322-68057372	A549	lung:	n/a
13	chr3:68053371-68053421	Hepatocyte	liver:	n/a
14	chr3:68057357-68057407	RPTEC	kidney:	n/a
15	chr3:68057306-68057356	SK-N-MC	brain:	n/a
16	chr3:68057357-68057407	GM12891	blood:	n/a
17	chr3:68053949-68053999	HRE	kidney:	n/a
18	chr3:68057357-68057407	MCF-7	breast:	n/a
19	chr3:68053371-68053421	GM06990	blood:	n/a
20	chr3:68056706-68056756	H1-hESC	embryonic stem cell:	embryo
21	chr3:68056976-68057026	HAEpiC	amniotic membrane:	n/a
22	chr3:68047840-68047890	Hela-S3	cervix:	n/a
23	chr3:68056976-68057026	BE2_C	brain:	n/a
24	chr3:68057025-68057075	HAEpiC	amniotic membrane:	n/a
25	chr3:68053371-68053421	AG04450	lung:	fetal
26	chr3:68039483-68039533	AoSMC	blood vessel:	n/a
27	chr3:68039483-68039533	GM12878	blood:	n/a
28	chr3:68056706-68056756	AG04450	lung:	fetal
29	chr3:68056706-68056756	AG09319	gingival:	n/a
30	chr3:68060925-68060975	MCF-7	breast:	n/a
31	chr3:68056706-68056756	HCF	heart:	n/a
32	chr3:68053949-68053999	MCF-7	breast:	n/a
33	chr3:68053484-68053534	NHDF-neo	bronchial:	n/a
34	chr3:68053371-68053421	ProgFib	skin:	n/a
35	chr3:68053949-68053999	PANC-1	pancreas:	n/a
36	chr3:68060925-68060975	GM12878	blood:	n/a
37	chr3:68053484-68053534	MCF-7	breast:	n/a
38	chr3:68056976-68057026	SAEC	small airway:	n/a
39	chr3:68053484-68053534	SAEC	small airway:	n/a
40	chr3:68053371-68053421	HRE	kidney:	n/a
41	chr3:68056706-68056756	SKMC	muscle:	n/a
42	chr3:68053484-68053534	NT2-D1	testis:	n/a
43	chr3:68039483-68039533	IMR90	lung:	fetal
44	chr3:68057025-68057075	GM12878	blood:	n/a
45	chr3:68053371-68053421	LNCaP	prostate:	n/a
46	chr3:68057322-68057372	Jurkat	blood:	n/a
47	chr3:68053371-68053421	RPTEC	kidney:	n/a
48	chr3:68056976-68057026	AG09309	skin:	n/a
49	chr3:68057025-68057075	AoSMC	blood vessel:	n/a
50	chr3:68057322-68057372	GM12892	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:68045575..68047988-chr3:68059342..68060872,2	MCF-7	breast:
2	chr3:67952201..67952773-chr3:68925063..68925992,2	MCF-7	breast:
3	chr3:67951890..67952870-chr3:68066397..68066948,2	MCF-7	breast:
4	chr3:67991094..67994023-chr3:67995213..67998211,2	MCF-7	breast:
5	chr3:68045575..68047988-chr3:68059342..68060872,2	MCF-7	breast:
6	chr3:67991094..67994023-chr3:67995213..67998211,2	MCF-7	breast:
7	chr3:67991529..67993327-chr3:67994469..67996433,2	MCF-7	breast:
8	chr3:68058440..68060357-chr3:68076381..68078551,2	K562	blood:
9	chr3:67951881..67952772-chr3:68305559..68306337,2	MCF-7	breast:
10	chr3:67951814..67952581-chr3:68255379..68256164,2	MCF-7	breast:
11	chr3:67991529..67993327-chr3:67994469..67996433,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM19A1-1	chr3:67939433-67939460	NONHSAT090326
2	lnc-FAM19A1-1	chr3:67939434-67939460	XLOC_002693
3	lnc-FAM19A1-1	chr3:67997565-67998136	NR_109992
4	lnc-FAM19A1-1	chr3:67939434-67939533	NR_109992
5	lnc-FAM19A1-1	chr3:67939434-67939533	ENSG00000241316
6	lnc-FAM19A1-1	chr3:67997565-67998137	ENSG00000241316

No data

Variant related genes	Relation type
FAM19A1	TF binding region
FAM19A1	CpG island
E2F3	miRNA target sites

Extended variants
information (count: 2327 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2327 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564211649	chr3:67925912-67925913	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs558060503	chr3:67925917-67925918	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs11711015	chr3:67925920-67925921	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs536610657	chr3:67925929-67925930	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs73837226	chr3:67925959-67925960	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs573612267	chr3:67926017-67926018	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs542746273	chr3:67926030-67926031	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs377304293	chr3:67926111-67926112	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs559581335	chr3:67926118-67926119	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs573100563	chr3:67926143-67926144	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs545308264	chr3:67926147-67926148	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs146449461	chr3:67926218-67926219	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs191728725	chr3:67926220-67926221	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs56087100	chr3:67926231-67926232	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs549858650	chr3:67926236-67926237	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs140843982	chr3:67926241-67926242	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs546981800	chr3:67926250-67926251	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs184320115	chr3:67926341-67926342	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs144603041	chr3:67926360-67926361	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs565508240	chr3:67926373-67926374	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs565915656	chr3:67926385-67926386	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs534924163	chr3:67926466-67926467	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs186789130	chr3:67926468-67926469	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs1485340	chr3:67926488-67926489	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs537756072	chr3:67926562-67926563	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs192721673	chr3:67926576-67926577	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs140359907	chr3:67926639-67926640	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs552875040	chr3:67926648-67926649	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs150353970	chr3:67926649-67926650	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs557929181	chr3:67926660-67926661	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs200842772	chr3:67926673-67926674	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs553138386	chr3:67926768-67926769	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs13072764	chr3:67926772-67926773	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs557351977	chr3:67926779-67926780	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs62254940	chr3:67926816-67926817	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs185410110	chr3:67926833-67926834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575409516	chr3:67926841-67926842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113378817	chr3:67926944-67926945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374812775	chr3:67927002-67927003	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139129526	chr3:67927015-67927016	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143047894	chr3:67927032-67927033	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375547545	chr3:67927036-67927037	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs573429721	chr3:67927056-67927057	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549052682	chr3:67927094-67927095	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs190710223	chr3:67927125-67927126	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370342826	chr3:67927131-67927132	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528586765	chr3:67927197-67927198	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181622956	chr3:67927205-67927206	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs113873141	chr3:67927351-67927352	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs144658118	chr3:67927362-67927363	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	21509527	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Prostate cancer	17217626	CNVD
Urothelial cell carcinoma	18451213	CNVD
Alzheimer''s disease	22166940	CNVD
Mental retardation	20848658	CNVD
Breast cancer	17142309	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:67925400-67927000	Enhancers	Liver	Liver
2	chr3:67925400-67927600	Enhancers	HepG2	liver
3	chr3:67925600-67926000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr3:67925600-67926800	Enhancers	Hela-S3	cervix
5	chr3:67925800-67926400	Flanking Active TSS	A549	lung
6	chr3:67925800-67937400	Weak transcription	Aorta	Aorta
7	chr3:67926000-67926400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr3:67926400-67926600	Active TSS	A549	lung
9	chr3:67926400-67927000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr3:67926400-67927000	Enhancers	Ovary	ovary
11	chr3:67926400-67928000	Enhancers	Fetal Intestine Large	intestine
12	chr3:67926600-67926800	Flanking Active TSS	A549	lung
13	chr3:67926600-67927200	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr3:67926600-67928000	Enhancers	Fetal Intestine Small	intestine
15	chr3:67927000-67927400	Flanking Active TSS	Liver	Liver
16	chr3:67927200-67927600	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr3:67927400-67928000	Enhancers	Liver	Liver
18	chr3:67927600-67928000	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr3:67934400-67934800	Enhancers	Fetal Brain Female	brain
20	chr3:67946200-67947400	Enhancers	Fetal Intestine Small	intestine
21	chr3:67946200-67947600	Enhancers	Fetal Intestine Large	intestine
22	chr3:67946400-67946600	Enhancers	Fetal Brain Male	brain
23	chr3:67946400-67947800	Enhancers	Liver	Liver
24	chr3:67946600-67947200	Weak transcription	Fetal Brain Male	brain
25	chr3:67947200-67948600	Enhancers	Fetal Brain Male	brain
26	chr3:67948000-67948400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr3:67948000-67948800	Enhancers	Fetal Kidney	kidney
28	chr3:67948000-67949600	Enhancers	Fetal Brain Female	brain
29	chr3:67948200-67948800	Enhancers	Primary B cells from peripheral blood	blood
30	chr3:67949200-67949600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr3:67956400-67957400	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr3:67956400-67958200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr3:67956600-67957200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr3:67956600-67957400	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr3:67956600-67957600	Enhancers	Primary hematopoietic stem cells	blood
36	chr3:67956600-67958000	Enhancers	Primary T cells from cord blood	blood
37	chr3:67956600-67958000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr3:67956800-67957200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr3:67956800-67957200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
40	chr3:67956800-67957600	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr3:67956800-67957800	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr3:67957400-67957600	Enhancers	Primary T cells fromperipheralblood	blood
43	chr3:67958000-67958400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:67958000-67958400	Enhancers	Brain Substantia Nigra	brain
45	chr3:67966000-67966800	Enhancers	Colon Smooth Muscle	Colon
46	chr3:67966800-67967200	Enhancers	Stomach Smooth Muscle	stomach
47	chr3:67969800-67972600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr3:67971200-67971800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr3:67971400-67971600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr3:67971600-67975600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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